FDA UDI In Commercial Distribution 🇺🇸 United States

3D-CA

DI: 00884838084773 · Model: 3D-CA - 3 · Philips Medical Systems Nederland B.V.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
3D-CA
Primary DI
00884838084773
Version / Model
3D-CA - 3
Catalog Number
001109
Company Name
Philips Medical Systems Nederland B.V.
Labeler DUNS
413819707
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-28
Public Version
9
Public Version Date
2023-09-26
Public Version Status
Update
Public Device Record Key
55a9665f-c5a7-4bf2-b947-9747dec645b7

Device Description

Software medical device, used with a Philips Interventional X-Ray System. Creates a 3D model of the coronary vessel tree from a pair of 2D images from a rotational angiographic run.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LLZ System, Image Processing, Radiological
IZI System, X-Ray, Angiographic

GMDN Terms

Code Name
40868 Angiographic x-ray system application software

Identifiers

Type ID
Primary 00884838084773

Premarket Submissions

Submission Number Supplement Number
K042334 000